Canonical Allele Identifier: CA1723632235

Gene: ABCB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87531261_87531265delinsCTTAA , CM000669.2:g.87531261_87531265delinsCTTAA	GRCh38
NC_000007.13:g.87160577_87160581delinsCTTAA , CM000669.1:g.87160577_87160581delinsCTTAA	GRCh37
NC_000007.12:g.86998513_86998517delinsCTTAA	NCBI36
NG_011513.1:g.186984_186988delinsTTAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.2685+29_2685+33delinsTTAAG	ENSP00000265724.3:n.2685+29_2685+33delinsTTAAG
ENST00000622132.5:c.2685+29_2685+33delinsTTAAG MANE Select	ENSP00000478255.1:n.2685+29_2685+33delinsTTAAG
ENST00000265724.7:c.2685+29_2685+33delinsTTAAG	ENSP00000265724.3:n.2685+29_2685+33delinsTTAAG
ENST00000488737.6:n.327+29_327+33delinsTTAAG
ENST00000496821.5:n.313+29_313+33delinsTTAAG
ENST00000543898.5:c.2493+29_2493+33delinsTTAAG	ENSP00000444095.1:n.2493+29_2493+33delinsTTAAG
ENST00000622132.4:c.2685+29_2685+33delinsTTAAG	ENSP00000478255.1:n.2685+29_2685+33delinsTTAAG
NM_000927.4:c.2685+29_2685+33delinsTTAAG	NP_000918.2:n.2685+29_2685+33delinsTTAAG
NM_001348944.1:c.2685+29_2685+33delinsTTAAG	NP_001335873.1:n.2685+29_2685+33delinsTTAAG
NM_001348945.1:c.2895+29_2895+33delinsTTAAG	NP_001335874.1:n.2895+29_2895+33delinsTTAAG
NM_001348946.1:c.2685+29_2685+33delinsTTAAG	NP_001335875.1:n.2685+29_2685+33delinsTTAAG
NM_001348946.2:c.2685+29_2685+33delinsTTAAG MANE Select	NP_001335875.1:n.2685+29_2685+33delinsTTAAG
NM_000927.5:c.2685+29_2685+33delinsTTAAG	NP_000918.2:n.2685+29_2685+33delinsTTAAG
NM_001348944.2:c.2685+29_2685+33delinsTTAAG	NP_001335873.1:n.2685+29_2685+33delinsTTAAG
NM_001348945.2:c.2895+29_2895+33delinsTTAAG	NP_001335874.1:n.2895+29_2895+33delinsTTAAG